Prenatal Diagnosis of WAGR Syndrome

الملخص EN

Wilm’s tumour, aniridia, genitourinary abnormalities, and mental retardation (WAGR) syndrome is a rare genetic disorder with an estimated prevalence of 1 in 500,000 to 1 million.

It is a contiguous gene syndrome due to deletion at chromosome 11p13 in a region containing WT1 and PAX6 genes.

Children with WAGR syndrome mostly present in the newborn/infancy period with sporadic aniridia.

The genotypic defects in WAGR syndrome have been well established.

However, antenatal ultrasonographic presentation of this syndrome has never been reported.

Prenatal diagnosis of this condition is possible in some cases with careful ultrasound examination of classical and nonclassical manifestations of this syndrome.

The key point for this rare diagnosis was the decision to perform chromosomal microarray analysis after antenatal diagnosis of absent corpus callosum and absent cavum septum pellucidum, as this finding mandates search for potentially associated genetic disorders.

We report a case of WAGR syndrome diagnosed prenatally at 29-week gestation.

The diagnosis of the anomaly was based on two- and three-dimensional ultrasound as well as fetal MRI scan and microarray analysis.

The ultrasonographic findings included borderline ventriculomegaly, absent corpus callosum, and absent cavum septum pellucidum.

Cytogenetic results from the amniotic fluid confirmed WAGR syndrome.

Parental karyotype was normal, with no evidence of copy number change, deletion, or rearrangement of this region of chromosome 11.